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Top Les Turner ALS Foundation News

Donald Trump · United States

New Car Tax Deduction Targets Interest on American-Made Vehicles

Coverage: 5 sources

The tax cut and spending package that was signed into law last week includes a tax deduction for interest on American-made vehicles.See the Story

Maryland · Maryland

LETTER: Advocating for the Renewal of ALLFTD Study to Propel ALS and FTD Research - Les Turner ALS Foundation

The Honorable Richard Hodes, MD, Director of the National Institute on Aging The Honorable Walter Koroshetz, MD, Director of the National Institute of Neurological Disorders and StrokeNational Institutes of Health 9000 Rockville Pike, Bethesda, Maryland 20892 Subject: ALLFTD Renewal Dear Dr. ... Read More The post LETTER: Advocating for the Renewal of ALLFTD Study to Propel ALS and FTD Research appeared first on Les Turner ALS Foundation.Read Article

ALS Awareness Month: Crossing the Rainbow: A Son’s Reflection on Caregiving and ALS - Les Turner ALS Foundation

A moving reflection from a son who cared for his mother through her ALS diagnosis. This essay explores the emotional weight of caregiving, the challenges of ALS, and the quiet power of love and dignity at the end of life.Chicago, IL · Chicago Read Article

ALS Awareness Month: "My mom's diagnosis broke my heart." - Les Turner ALS Foundation

For ALS Awareness Month, we asked members of the Les Turner ALS Foundation’s Support Services Committee to help us explore topics in ALS that people should know more about. For the second week of May, we’re looking at diagnostic delays, which are ... Read More The post ALS Awareness Month: “My mom’s diagnosis broke my heart.” appeared first on Les Turner ALS Foundation.Chicago, IL · Chicago Read Article

ALS Awareness Month: “I Knew Something Was Wrong”— Stories of Delayed ALS Diagnosis - Les Turner ALS Foundation

Discover the real stories of Janie and Barbara, two women living with ALS, as they share their experiences navigating delayed diagnoses. Learn why early detection matters and how the Les Turner ALS Foundation is advocating for faster, more accurate ALS diagnosis.Chicago, IL · Chicago Read Article

ALS Awareness Month: A Mother’s Day Reflection Balancing ALS and Motherhood - Les Turner ALS Foundation

For ALS Awareness Month, we asked members of the Les Turner ALS Foundation’s Support Services Committee to help us explore topics in ALS that people should know more about. For the first week of May, we’re looking at a day in the ... Read More The post ALS Awareness Month: A Mother’s Day Reflection Balancing ALS and Motherhood appeared first on Les Turner ALS Foundation.Skokie · Skokie Read Article

B.C. couple launches grueling ALS fundraising journey in Nanaimo

NANAIMO — Competing in triathlons across the country won’t be easy, but a Vernon couple has motivation on their side. Mike Pearson, 63, and Donna Bartel, 59, start Trii’ing to End ALS (Amyotrophic Lateral Sclerosis) on Sunday, May 11 at Nanaimo’s Westwood Lake Park. The devastating progressive, often fatal neurological disease affects brain and spinal cord nerve cells, leading to increasingly restrictive muscle control. ALS claimed the life of P…Nanaimo · Nanaimo See the Story

Faces of ALS: Jim Halstead, A life of joyful fidelity - Les Turner ALS Foundation

At 76, Jim Halstead faces ALS with grace and reflection. Read how a priest and professor continues to lead, connect, and inspire through his journey.Chicago, IL · Chicago Read Article

Aim for 2025 ALS Awareness Month is to amplify community voices

Across the U.S. and around the world, the amyotrophic lateral sclerosis (ALS) community is aiming to raise its voice in powerful ways this May during awareness month — with advocacy campaigns, flag displays, the sharing of personal stories, and community-led events. ALS Awareness Month, according to supporters of those with the neuromuscular condition, is an opportunity to shine a light on the lives touched by ALS and to advance efforts to impr…Illinois · Illinois See the Story

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News from Les Turner ALS Foundation

News from Les Turner ALS Foundation